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rs387907026

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907026(C;T)
Make rs387907026(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position967282
GeneRSPO4
is asnp
is mentioned by
dbSNPrs387907026
ebirs387907026
HLIrs387907026
Exacrs387907026
Varsomers387907026
Maprs387907026
PheGenIrs387907026
hapmaprs387907026
1000 genomesrs387907026
hgdprs387907026
ensemblrs387907026
gopubmedrs387907026
geneviewrs387907026
scholarrs387907026
googlers387907026
pharmgkbrs387907026
gwascentralrs387907026
openSNPrs387907026
23andMers387907026
23andMe allrs387907026
SNP Nexus

SNPshotrs387907026
SNPdbers387907026
MSV3drs387907026
GWAS Ctlgrs387907026
Max Magnitude0
ClinVar
Risk rs387907026(T;T)
Alt rs387907026(T;T)
Reference rs387907026(C;C)
Significance Pathogenic
Disease Anonychia
Variation info
Gene RSPO4
CLNDBN Anonychia
Reversed 1
HGVS NC_000020.10:g.947925G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023830.2,